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PHARMA-PLAST PURELINE(TM) BASIC(TM) AND PURELINE(TM) CONTACT(TM) SUBCUTANEOUS INFUSION SETS

Page Type
Cleared 510(K)
510(k) Number
K945617
510(k) Type
Traditional
Applicant
PHARMA-PLAST INTL. A/S
Country
Denmark
FDA Decision
Substantially Equivalent
Decision Date
2/13/1995
Days to Decision
90 days
Submission Type
Summary

PHARMA-PLAST PURELINE(TM) BASIC(TM) AND PURELINE(TM) CONTACT(TM) SUBCUTANEOUS INFUSION SETS

Page Type
Cleared 510(K)
510(k) Number
K945617
510(k) Type
Traditional
Applicant
PHARMA-PLAST INTL. A/S
Country
Denmark
FDA Decision
Substantially Equivalent
Decision Date
2/13/1995
Days to Decision
90 days
Submission Type
Summary